Natco Pharma’s partner gets US FDA nod for cancer treatment drug

Natco Pharma said its marketing partner Breckenridge Pharmaceutical has received final approval from the US health regulator for pomalidomide capsules, treatment of patients suffering from multiple myeloma cancer.


Breckenridge Pharmaceutical has received final approval for its abbreviated new drug application (ANDA) for Pomalidomide Capsules from the US Food and Drug Administration (US FDA),” Natco Pharma said in a regulatory filing.

In addition, Natco and Breckenridge have settled the patent litigation with Celgene (now part of Bristol-Myers Squibb) in the US district court for this product, the company added.

The company, however, did not share details of the settlement.

Celgene sells Pomalidomide Capsules under Brand name Pomalyst in the US market which is indicated for the treatment of patients suffering from multiple myeloma cancer.

Natco Pharma said as per industry sales data, Pomalyst had annual sales of $957 million during the twelve months ending September 2020.

Source:https://indiamedtoday.com/natco-pharmas-partner-gets-us-fda-nod-for-cancer-treatment-drug/

Comments

Popular posts from this blog

EMA validates Incyte’s MAA for retifanlimab to treat metastatic squamous cell anal carcinoma

Merck’s Keytruda plus platinum- and fluoropyrimidine-based chemotherapy receives US FDA nod to treat certain patients with locally advanced/metastatic esophageal or GEJ carcinoma

Tumour-targeting drug paves way for bone cancer treatment